RX-5902 Treatment of Subjects With Triple Negative Breast Cancer

Status Terminated

Clinical Trial Summary

The purpose of this Phase 2 portion of the study is to use the dose and schedule of RX-5902 identified in the phase 1 to treat subjects with triple negative breast cancer.

Clinical Trial Description

In this dose-finding, open-label, single-agent study of RX-5902, subjects will be treated for up to 6 cycles of therapy. RX-5902 will be administered orally daily for 3 weeks followed by 1 week of rest in each cycle. All subjects will be followed for at least 30 days after the last dose of study agent for safety. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02003092
Study type	Interventional
Source	Rexahn Pharmaceuticals, Inc.
Contact
Status	Terminated
Phase	Phase 1/Phase 2
Start date	August 2013
Completion date	November 2019

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